Q44.70
BillableOther congenital malformation of liver, unspecified
Other congenital malformation of liver, unspecified
Status
Billable / Specific
Parent Code
Q44.7Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital malformation of liver, NOS
Excludes 2
Conditions not included here, but the patient may have both
Code Also
A second code may be required; sequencing depends on circumstances
- , if applicable, associated malformations affecting other systems
Related Codes(2)
Also Known As / Clinical Terms(55)
SNOMED CT
- Congenital anomaly of liver89166001
- Congenital malformation of liver89166001
- Congenital abnormality of liver and/or biliary tract268213006
- Liver and biliary system anomalies268213006
- Cone dystrophy312917007
- Fatal infantile diarrhea with trichorrhexis nodosa703406006
- Fatal infantile diarrhoea with trichorrhexis nodosa703406006
- Intractable diarrhea with phenotypic anomalies703406006
- Intractable diarrhoea with phenotypic anomalies703406006
- Phenotypic diarrhea of infancy703406006
- Phenotypic diarrhoea of infancy703406006
- Syndromic diarrhea703406006
- Syndromic diarrhoea703406006
- Tricho-hepato-enteric syndrome703406006
- Trichohepatoenteric syndrome703406006
- RHE (retinohepatoendocrinologic) syndrome724000006
- RHE syndrome724000006
- Retinohepatoendocrinologic syndrome724000006
- Mitochondrial DNA depletion syndrome hepatocerebrorenal form782771007
- Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form782771007
- Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency783734000
- Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency783734000
- Navajo neurohepatopathy784346006
- Navajo neuropathy784346006
UMLS
Clinical Terms
- Mitochondrial DNA depletion syndrome hepatocerebrorenal form
- Congenital malformation of liver, NOS
- Phenotypic diarrhoea of infancy
- Navajo neuropathy
- Liver and biliary system anomalies
- RHE syndrome
- Congenital anomaly of liver (disorder)
- Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency
- RHE (retinohepatoendocrinologic) syndrome
- Cone dystrophy
- Intractable diarrhea with phenotypic anomalies
- Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form
- Fatal infantile diarrhoea with trichorrhexis nodosa
- Tricho-hepato-enteric syndrome
- Intractable diarrhoea with phenotypic anomalies
- Phenotypic diarrhea of infancy
- Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
- Syndromic diarrhea
- Congenital anomaly of liver
- Retinohepatoendocrinologic syndrome
- Congenital abnormality of liver and/or biliary tract
- Syndromic diarrhoea
- Trichohepatoenteric syndrome
- Fatal infantile diarrhea with trichorrhexis nodosa
- Congenital malformation of liver
- Navajo neurohepatopathy
Frequently Asked Questions
What is the ICD-10 code for other congenital malformation of liver, unspecified?
The ICD-10-CM code for other congenital malformation of liver, unspecified is Q44.70. The full clinical description is "Other congenital malformation of liver, unspecified". Q44.70 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q44.70 mean?
ICD-10-CM code Q44.70 represents “Other congenital malformation of liver, unspecified”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q44.70 a billable code?
Yes, Q44.70 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q44.70 in?
Q44.70 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q44.70 map to?
Q44.70 maps to 8 SNOMED CT concepts: 312917007, 268213006, 89166001, 703406006, 782771007, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q44.70?
Q44.70 is linked to 2 UMLS Concept Unique Identifiers: C0266257, C5819272. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q44.70 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformation of liver, unspecified affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q44.70?
There is no direct ICD-11 mapping available for Q44.70 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.